Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:97498809-97499117 | Rare:88 | ||||
chr10:97633430-97633636 | Common:2; Rare:52 | ||||
chr10:98446797-98447045 | Rare:70; Clinvar:1 | ||||
chr10:99430616-99430957 | Common:3; Rare:82 | ||||
chr10:99659224-99659574 | Common:2; Rare:92 | ||||
chr10:99731976-99732384 | Common:1; Rare:153; Clinvar:5; Clinvar (benign):1 | ||||
chr10:100185938-100186085 | Rare:58 | ||||
chr10:100229547-100229668 | Rare:42 | ||||
chr10:100267569-100267757 | Common:3; Rare:66 | ||||
chr10:100286559-100286725 | Common:4; Rare:89 | ||||
chr10:100536070-100536658 | Common:3; Rare:129 | ||||
chr10:100912770-100913002 | Common:1; Rare:66 | ||||
chr10:100913321-100913417 | Rare:28 | ||||
chr10:100987330-100987863 | Common:2; Rare:155; Clinvar:3; Clinvar (benign):2 | ||||
chr10:101031098-101031522 | Common:1; Rare:98 |